Consensus recommendations for hyperpolarized [1‐ <scp> <sup>13</sup> C </scp> ]pyruvate <scp>MRI</scp> multi‐center human studies
Shonit Punwani, Peder E. Z. Larson, Christoffer Laustsen, Jan VanderMeulen, Jan Henrik Ardenkjær‐Larsen, Adam W. Autry, James A. Bankson, Jenna Bernard, Robert Bok, Lotte Bonde Bertelsen, Jenny Che, Albert P. Chen, Rafat Chowdhury, Arnaud Comment, Charles H. Cunningham, Duy Dang, Ferdia A. Gallagher, Adam Gaunt, Yangcan Gong, Jeremy W. Gordon, Ashley Grimmer, James T. Grist, Esben Søvsø Szocska Hansen, Mathilde H. Lerche, Richard L. Hesketh, Jan‐Bernd Hoevener, Ching‐Yi Hsieh, Kayvan R. Keshari, Kozerke Sebastian, Titus Lanz, Dirk Mayer, Mary A. McLean, Jae Mo Park, Jim Slater, Damian J. Tyler, Jean‐Luc Vanderheyden, Cornelius von Morze, Fulvio Zaccagna, Vlad G. Zaha, Duan Xu, Daniel B. Vigneron, The HP 13C MRI Consensus Group
Abstract
Abstract MRI of hyperpolarized (HP) [1‐ 13 C]pyruvate allows in vivo assessment of metabolism and has translated into human studies across diseases at 15 centers worldwide. To determine consensus on best practice for multi‐center studies for development of clinical applications. This paper presents the results of a two‐round formal consensus building exercise carried out by experts with HP [1‐ 13 C]pyruvate human study experience. Twenty‐nine participants from 13 sites brought together expertise in pharmacy methods, MR physics, translational imaging, and data analysis with the goal of providing recommendations and best practice statements on conduct of multi‐center human studies of HP [1‐ 13 C]pyruvate MRI. Overall, the group reached consensus on approximately two‐thirds of 246 statements in the questionnaire, covering HP 13 C‐pyruvate preparation; MRI system setup, calibration, and phantoms; acquisition and reconstruction; and data analysis and quantification. Consensus was present across categories. Examples include: (i) Different HP pyruvate preparation methods could be used in human studies, but the same release criteria have to be followed; (ii) site qualification and quality assurance must be performed with phantoms and the same field strength must be used, but the rest of the system setup and calibration methods could be determined by individual sites; (iii) the same pulse sequence and reconstruction methods were preferable, but the exact choice should be governed by the anatomical target; (iv) normalized metabolite area‐under‐curve values and metabolite area under curve were the preferred metabolism metrics. The consensus proces revealed that HP[1‐ 13 C] pyruvate MRI as a technology has progressed sufficiently to plan multi‐center studies. The work confirmed areas of consensus for multi‐center study conduct and identified where further research is required to ascertain best practice.